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Applied and Environmental Microbiology, October 2003, p. 6225-6234, Vol. 69, No. 10
0099-2240/03/$08.00+0     DOI: 10.1128/AEM.69.10.6225-6234.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Spiralin Is Not Essential for Helicity, Motility, or Pathogenicity but Is Required for Efficient Transmission of Spiroplasma citri by Its Leafhopper Vector Circulifer haematoceps

Sybille Duret, Nathalie Berho, Jean-Luc Danet, Monique Garnier, and Joël Renaudin*

UMR Génomique Développement et Pouvoir Pathogène, IBVM, Centre INRA de Bordeaux, 33883 Villenave d'Ornon Cedex, France

Received 7 April 2003/ Accepted 15 July 2003

Spiralin is the most abundant protein at the surface of the plant pathogenic mollicute Spiroplasma citri and hence might play a role in the interactions of the spiroplasma with its host plant and/or its insect vector. To study spiralin function, mutants were produced by inactivating the spiralin gene through homologous recombination. A spiralin-green fluorescent protein (GFP) translational fusion was engineered and introduced into S. citri by using an oriC-based targeting vector. According to the strategy used, integration of the plasmid by a single-crossover recombination at the spiralin gene resulted in the expression of the spiralin-GFP fusion protein. Two distinct mutants were isolated. Western and colony immunoblot analyses showed that one mutant (GII3-9a5) did produce the spiralin-GFP fusion protein, which was found not to fluoresce, whereas the other (GII3-9a2) produced neither the fusion protein nor the wild-type spiralin. Both mutants displayed helical morphology and motility, similarly to the wild-type strain GII-3. Genomic DNA analyses revealed that GII3-9a5 was unstable and that GII3-9a2 was probably derived from GII3-9a5 by a double-crossover recombination between plasmid sequences integrated into the GII3-9a5 chromosome and free plasmid. When injected into the leafhopper vector Circulifer haematoceps, the spiralinless mutant GII3-9a2 multiplied to high titers in the insects (1.1 x 106 to 2.8 x 106 CFU/insect) but was transmitted to the host plant 100 times less efficiently than the wild-type strain. As a result, not all plants were infected, and symptom production in these plants was delayed for 2 to 4 weeks compared to that in the wild-type strain. In the infected plants however, the mutant multiplied to high titers (1.2 x 106 to 1.4 x 107 CFU/g of midribs) and produced the typical symptoms of the disease. These results indicate that spiralin is not essential for pathogenicity but is required for efficient transmission of S. citri by its insect vector.

* Corresponding author. Mailing address: UMR GDPP, IBVM, Centre INRA de Bordeaux, 71 avenue Edouard Bourlaux, B.P. 81, 33883 Villenave d'Ornon Cedex, France. Phone: (33) 5.57.12.23.61. Fax: (33) 5.57.12.23.69. E-mail: renaudin{at}bordeaux.inra.fr.

Applied and Environmental Microbiology, October 2003, p. 6225-6234, Vol. 69, No. 10
0099-2240/03/$08.00+0     DOI: 10.1128/AEM.69.10.6225-6234.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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